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Ferreira, Franck; Denichoux, Aurélien; Chemla, Fabrice; Bejjani, Joseph (2004). "Highly
Diastereoselective Syntheses of Propargylic Acid and Homopropargylic Systems".
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a saturated position on a molecular framework next to a propargylic group and thus two bonds from an
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99:, which refers to the typical reaction of the terminal alkynes with
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23:Chemical structure of the propargyl group.
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87:) on a molecular framework next to an
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91:group. The name comes from mix of
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110:designates in the same manner
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133:, or substituted homologue.
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16:Chemical group (–CH₂C≡CH)
121:a 3-butynyl fragment,
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212:10.1055/s-2004-832816
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237:Propargyl compounds
58:group derived from
166:Propargyl chloride
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242:Functional groups
206:(12): 2051–2065.
176:Propargyl bromide
171:Propargyl alcohol
29:organic chemistry
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37:functional group
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108:homopropargylic
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33:propargyl group
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232:Alkynyl groups
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181:Propiolic acid
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144:Alkenyl groups
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101:silver salts
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154:Vinyl group
85:-hybridized
74:propargylic
54:. It is an
226:Categories
187:References
80:position (
106:The term
78:saturated
72:The term
45:structure
43:with the
138:See also
97:argentum
41:propynyl
203:Synlett
161:Ethynyl
123:HC≡C−CH
118:moiety.
93:propene
89:alkynyl
64:HC≡C−CH
60:propyne
48:CH≡C−CH
116:alkyne
31:, the
149:Allyl
56:alkyl
39:of 2-
35:is a
95:and
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27:In
228::
127:CH
103:.
83:sp
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131:−
129:2
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62:(
52:−
50:2
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